Product Details

SNP ID
rs199890965
Assay Type
Functionally Tested
NCBI dbSNP Submissions
5
Location
Chr.1:117957169 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CAGCTGGGCTCTGATGTTGAACTTA[G/T]ATGCCGGTGCCTCTTCTTCCTCCTT
Phenotype
MIM: 616554 MIM: 604737
Polymorphism
G/T, Transversion Substitution
Allele Nomenclature
Literature Links
SPAG17 PubMed Links

Gene Details

Gene
SPAG17
Gene Name
sperm associated antigen 17
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_206996.2 2621 Intron NP_996879.1
XM_006710426.3 2621 Intron XP_006710489.1
XM_006710427.3 2621 Intron XP_006710490.1
XM_006710428.3 2621 Intron XP_006710491.1
XM_006710429.3 2621 Intron XP_006710492.1
XM_006710431.3 2621 Intron XP_006710494.1
XM_011540934.1 2621 Intron XP_011539236.1
XM_011540935.2 2621 Intron XP_011539237.1
XM_011540936.2 2621 Intron XP_011539238.1
XM_011540937.2 2621 Intron XP_011539239.1
XM_011540939.2 2621 Intron XP_011539241.1
XM_011540941.2 2621 Intron XP_011539243.1
XM_011540942.2 2621 Intron XP_011539244.1
Gene
WDR3
Gene Name
WD repeat domain 3
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_006784.2 2621 Missense Mutation AGA,ATA R852I NP_006775.1

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